Senior Migration Consultant - Clinical Data Programming

Veeva Systems; Marbella; Remote; EUR 80,000 - 125,000; Full time

Job summary

Cytel seeks a Senior/Principal Statistical Programmer to work remotely with a pharmaceutical client, driving data analysis and reporting. You will implement SDTM/ADaM specifications, create datasets, reviewer’s guides and define.xml, and develop SAS programs for complex listings and graphs.

You will oversee CRO programming deliverables, ensure timely, high-quality results, and provide expert technical support to the biostatistics and programming team across studies.

Qualifications

• Experience delivering SDTM/ADaM specifications and datasets.
• Strong SAS and R programming for listings, tables, and graphs.
• Ability to supervise CRO programming deliverables.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
• Develop SAS programs which generate datasets, complex listings, tables and graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs
• Oversee CRO's statistical programming deliverables for multiple clinical studies to ensure quality and timelines
• Provide technical support to the team across studies

Skills

SAS programming

R programming

Clinical trial data analysis

Leadership

Education

Bachelor's degree in Biostatistics

Tools

SAS

R

SDTM

ADaM

Define.xml

Job description

Senior/Principal Statistical Programmer SAS + R (Remote)

**Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

**Position Overview:** This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.

**As a Principal Statistical Programmer, your responsibilities will include:**

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
• Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
• Support